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Filtered Search Results
Medchemexpress LLC Berubicin hydrochloride | 293736-67-1 | 95.1% | 670.10 | 1 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Berubicin hydrochloride is an analog of Doxorubicin that can cross the blood-brain barrier. It inhibits P-gp and MRP1-mediated efflux and suppresses glioblastoma multiforme (GBM). This product exerts toxic effects on leukemia cells by activating nuclear factor κB (NF-κB) and induces apoptosis in neuroblastoma cells. It can be used in the study of tumors related to the nervous system.
- Crosses the blood-brain barrier
- Inhibits P-gp and MRP1-mediated efflux
- Suppresses glioblastoma multiforme (GBM)
- Activates nuclear factor κB (NF-κB)
- Induces apoptosis in neuroblastoma cells
- More potent activity than Doxorubicin in activating NF-κB and inhibiting DNA synthesis
- Prolongs survival time in intracranial orthotopic glioma models in mice
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC mAChR-IN-1 (hydrochloride) | 119391-73-0 | 99.6% | 524.82 g/mol | C23H26ClIN2O2 | 10MM 1ML
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mAChR-IN-1 hydrochloride is a potent muscarinic cholinergic receptor antagonist (IC50 17 nM) provided for research use. It is offered as a solid and as a pre-made solution in DMSO, intended for in vitro pharmacology and receptor binding studies.
- Potent mAChR antagonist (IC50 17 nM).
- High purity: 99.6% (LCMS).
- Chemical formula: C23H26ClIN2O2.
- Molecular weight: 524.82 g/mol.
- Physical appearance: white to off-white solid.
- Available as solids (5-100 mg) and 10 mM solution in DMSO, 1 mL.
- Supplied for research use only.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Nifenalol hydrochloride | 5704-60-9 | 260.72 | C11H17ClN2O3 | 5 MG
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Nifenalol hydrochloride is a β-adrenergic receptor antagonist used in cardiac electrophysiology and pharmacology research. The compound is reported to induce early afterdepolarization (EAD) and is used to study arrhythmia and blood pressure-related effects.
- Beta-adrenergic receptor antagonist activity
- Induces early afterdepolarization useful for arrhythmia studies
- Hydrochloride salt form for improved solubility
- Molecular formula C11H17ClN2O3
- Molecular weight 260.72
- Available in small research pack sizes (e.g., 5 mg)
- Intended for in vitro and in vivo research applications
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Indotecan (hydrochloride) | 1228035-68-4 | 99.8% | 514.95 | 25 MG
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Indotecan hydrochloride, an indenoisoquinoline derivative, is a potent Topoisomerase I inhibitor. It has IC50s of 300, 1200, and 560 nM for P388, HCT116, and MCF-7 cell lines, respectively. This compound prevents the relaxation of supercoiled DNA and can be utilized for research on visceral leishmaniasis.
- Potent Topoisomerase I inhibitor.
- Effective in preventing relaxation of supercoiled DNA.
- Can be used for research on visceral leishmaniasis.
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Medchemexpress LLC CP-640186 (hydrochloride) | 591778-70-0 | C30H36ClN3O3 | 100 MG
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CP-640186 hydrochloride is an orally active and cell-permeable inhibitor of Acetyl-CoA carboxylase (ACC). It exhibits IC50 values of 53 nM for rat liver ACC1 and 61 nM for rat skeletal muscle ACC2. ACC is a crucial enzyme involved in fatty acid metabolism, responsible for synthesizing malonyl-CoA. This compound also promotes muscle fatty acid oxidation.
- Orally active and cell-permeable.
- Inhibits Acetyl-CoA carboxylase (ACC).
- IC50s: 53 nM for rat liver ACC1, 61 nM for rat skeletal muscle ACC2.
- Stimulates muscle fatty acid oxidation.
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Medchemexpress LLC Mefuparib hydrochloride | 1449746-00-2 | 98.6% | 334.77 | 5 MG
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Mefuparib hydrochloride is an orally active, substrate-competitive, and selective inhibitor of PARP1/2, with IC50 values of 3.2 nM and 1.9 nM respectively. It is known to induce apoptosis and exhibits significant anticancer activity both in vitro and in vivo.
- Orally active.
- Substrate-competitive and selective PARP1/2 inhibitor.
- Induces apoptosis.
- Possesses prominent anticancer activity in vitro and in vivo.
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Medchemexpress LLC Viloxazine hydrochloride | 35604-67-2 | MFCD00661100 | 98.9% | 273.75 g/mol | C13H20ClNO3 | 10MM 1ML
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Viloxazine hydrochloride is a research-grade small-molecule norepinephrine transporter inhibitor supplied for in vitro pharmacology and biochemical assays. The product is available as solid and as a ready-to-use 10 mM solution in DMSO (1 mL), providing a convenient format for concentration-controlled experiments.
- Ready-to-use 10 mM solution in DMSO, 1 mL
- Also available as solid in multiple mg pack sizes
- High purity (98.9% typical)
- Molecular formula C13H20ClNO3 and molecular weight ~273.75 g/mol
- CAS number 35604-67-2 for unambiguous identification
- SDS and storage instructions provided for safe handling
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Medchemexpress LLC Etifoxine hydrochloride | 56776-32-0 | 99.8% | 337.24 | 10 MM 1 ML
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Etifoxine hydrochloride is a non-benzodiazepine GABAergic compound. It acts as a positive allosteric modulator of α1β2γ2 and α1β3γ2 subunit-containing GABAA receptors. It has demonstrated anxiolytic and anticonvulsant properties in rodents.
- Acts as a positive allosteric modulator of GABAA receptors.
- Demonstrates anxiolytic properties.
- Demonstrates anticonvulsant properties.
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Medchemexpress LLC Noscapine (hydrochloride) | 912-60-7 | 99.9% | 449.88 | 250 MG
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Noscapine hydrochloride is an orally active phthalideisoquinoline alkaloid with potent antitussive effects. It activates sigma opioid receptors and inhibits Bradykinin non-competitively. It also disrupts microtubule dynamics, leading to mitotic arrest and apoptosis. This compound exhibits anticancer, neuroprotective, and anti-inflammatory activities, and can cross the blood-brain barrier.
- Activates sigma opioid receptors
- Non-competitive Bradykinin inhibitor
- Disrupts microtubule dynamics
- Induces mitotic arrest and apoptosis
- Exhibits anticancer activity
- Exhibits neuroprotective activity
- Exhibits anti-inflammatory activities
- Capable of crossing the blood-brain barrier
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Medchemexpress LLC Sri-37330 hydrochloride | 2322245-49-6 | 99.72% | C16H20ClF3N4O2S | 1 G
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SRI-37330 hydrochloride is an orally bioavailable thioredoxin-interacting protein (TXNIP) inhibitor. It inhibits glucagon secretion and function, reduces hepatic glucose production, and reverses hepatic steatosis. This compound can be used for type 2 diabetes research.
- Inhibits human TXNIP promoter activity in INS-1 cells.
- Decreases TXNIP mRNA and protein levels in INS-1 cells.
- Blocks polymerase II binding to the E-box motif of the TXNIP promoter.
- Reduces glucagon secretion in TC1-6 cells.
- Inhibits glucagon-induced glucose output from primary hepatocytes.
- Decreases glucagon secretion and action, and blocks hepatic glucose output in vivo.
- Well tolerated in male C57BL/6J mice.
- Reverses obesity- and STZ-induced diabetes and hepatic steatosis in mice.
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Medchemexpress LLC Fadrozole hydrochloride | 102676-31-3 | 99.9% | C14H14ClN3 | 1 ML
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Fadrozole hydrochloride (CGS 16949A) is a potent, selective, and nonsteroidal aromatase inhibitor that effectively inhibits estrogen production. It is intended for research use only and not for patient use.
- Potent and selective aromatase inhibitor with an IC50 of 6.4 nM.
- Inhibits estrogen production in hamster ovarian slices with an IC50 of 0.03 μM.
- Can suppress the synthesis of other cytochrome P-450 dependent steroids at higher doses.
- Prevents the development of spontaneous mammary neoplasms in female rats.
- Slows the development of pituitary pars distalis adenomas.
- Reduces the incidence of spontaneous hepatocellular tumors.
- Reduces parasite burden in male and female mice by 70%.
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Medchemexpress LLC AMXI-5001 hydrochloride | 98.1% | C25H21ClFN5O3 | 1 ML
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AMXI-5001 hydrochloride is a potent, orally active, and dual PARP1/2 and microtubule polymerization inhibitor. It shows selective antitumor cytotoxicity across a wide range of human cancer cells with significantly lower IC50s compared to existing clinical PARP1/2 inhibitors, and can induce complete regression of established tumors, including very large ones.
- Potent and orally active
- Dual PARP1/2 and microtubule polymerization inhibitor
- Selective antitumor cytotoxicity across a wide range of human cancer cells
- Significantly lower IC50s compared to existing clinical PARP1/2 inhibitors
- Induces complete regression of established tumors
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Medchemexpress LLC DC-BPi-11 hydrochloride | 97.0% | C20H24ClN5O2S | 1 ML
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DC-BPi-11 hydrochloride is an inhibitor of bromodomain PHD finger transcription factor (BPTF) with an IC50 of 698 nM. It significantly inhibits leukemia cell proliferation in human leukemia MV-4-11 cells (EC50 120 nM, IC50 0.89 μM). The compound decreases downstream oncogene expression and c-Myc protein levels, with minimal effects on normal cells. Intended for research use only.
- Inhibits bromodomain PHD finger transcription factor (BPTF)
- IC50 of 698 nM against BPTF
- Inhibits leukemia cell proliferation
- Decreases oncogene expression and c-Myc protein
- Minimal effects on normal cells
- Off-white to light yellow solid appearance
- Molecular weight: 433.95
- Chemical formula: C20H24ClN5O2S
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Medchemexpress LLC Melitracen hydrochloride | 10563-70-9 | MFCD00242905 | 99.8% | 327.89 g/mol | C21H26ClN | 1 ML
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Melitracen hydrochloride is a research-grade small molecule antidepressant and anxiolytic agent supplied for in vitro pharmacology, mechanism-of-action studies, and analytical reference. The material is provided with solubility and stock-solution guidance, and recommended storage conditions for both solid and solution forms.
- High purity of 99.8%.
- CAS number 10563-70-9, formula C21H26ClN, molecular weight 327.89 g/mol.
- Available as solid samples and as a pre-made 10 mM solution (1 mL) in DMSO.
- Soluble in DMSO and water at up to 100 mg/mL; ultrasonic assistance may be required.
- Storage: solid at 4°C; in solution store at -80°C up to 6 months or -20°C up to 1 month.
- Includes stock solution preparation guidance for common concentrations.
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Medchemexpress LLC SRI-37330 hydrochloride | 2322245-49-6 | 99.7% | C16H20ClF3N4O2S | 500 MG
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SRI-37330 hydrochloride is an orally bioavailable thioredoxin-interacting protein (TXNIP) inhibitor. It inhibits glucagon secretion and function, reduces hepatic glucose production, and reverses hepatic steatosis. This compound can be used for type 2 diabetes research.
- Inhibits human TXNIP promoter activity and reduces TXNIP mRNA and protein levels in INS-1 cells.
- Lowers glucagon secretion in TC1-6 cells and decreases glucagon secretion and action in vivo.
- Reduces glucagon-induced glucose output from primary hepatocytes and blocks hepatic glucose output in vivo.
- Reverses obesity- and Streptozotocin (STZ)-induced diabetes and hepatic steatosis in mice.
- Orally bioavailable.
- Well-tolerated in male C57BL/6J mice.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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